MedicineBiology

B. Haynes, M. A. Moody, L. Verkoczy, G. Kelsoe, S., Munir S. Alam

2005.8.1Human Antibodies

DOI: 10.3233/hab-2005-143-402

tlooto Summary

The hypothesis is that one reason antibodies against some of the conserved HIV-1 envelope trimer neutralizing epitopes are not routinely made may be down-regulation of some specificities of anti-HIV-1 antibody producing B cells by host B cell tolerance mechanisms.

Abstract

HIV-1 has evolved many ways to evade protective host immune responses, thus creating a number of problems for HIV vaccine developers. In particular, durable, broadly specific neutralizing antibodies to HIV-1 have proved difficult to induce with current HIV-1 vaccine candidates. The recent observation that some broadly neutralizing anti-HIV-1 envelope monoclonal antibodies have polyspecific reactivities to host antigens have raised the hypothesis that one reason antibodies against some of the conserved HIV-1 envelope trimer neutralizing epitopes are not routinely made may be down-regulation of some specificities of anti-HIV-1 antibody producing B cells by host B cell tolerance mechanisms.

Citation format

HAYNES, B., et al. Antibody polyspecificity and neutralization of HIV-1: A hypothesis. Human Antibodies, 2005, 14: 59–67.